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Linnankivi, Tarja
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1

Epilepsies with onset during the first year of life: A pros..:

Jonsson, Henna ; Gaily, Eija ; Stjerna, Susanna...
Epilepsia Open.  9 (2024)  4 - p. 1393-1405 , 2024
Link: https://doi.org/10.1002/..
 
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2

Missense variants in ANO4 cause sporadic encephalopathic or..:

Yang, Fang ; Begemann, Anais ; Reichhart, Nadine...
The American Journal of Human Genetics.  111 (2024)  6 - p. 1184-1205 , 2024
Link: https://doi.org/10.1016/..
 
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3

Corrigendum: Intrafamilial variability in SLC6A1-related ne..:

Kassabian, Benedetta ; Fenger, Christina Dühring ; Willems, Marjolaine...
Frontiers in Neuroscience.  17 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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4

Clinical and electrophysiological features of SCN8A variant..:

Lyu, Hang ; Boßelmann, Christian M. ; Johannesen, Katrine M....
eBioMedicine.  98 (2023)  - p. 104855 , 2023
Link: https://doi.org/10.1016/..
 
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5

Intrafamilial variability in SLC6A1-related neurodevelopmen..:

Kassabian, Benedetta ; Fenger, Christina Dühring ; Willems, Marjolaine...
Frontiers in Neuroscience.  17 (2023)  - p. , 2023
Link: https://doi.org/10.3389/..
 
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6

Networks of cortical activity in infants with epilepsy:

Auno, Sami ; Jonsson, Henna ; Linnankivi, Tarja..
Brain Communications.  4 (2022)  6 - p. , 2022
Link: https://doi.org/10.1093/..
 
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7

Visual field defects after vigabatrin treatment during infa..:

Jonsson, Henna ; Lehto, Mikko ; Vanhatalo, Sampsa..
Developmental Medicine & Child Neurology.  64 (2021)  5 - p. 641-648 , 2021
Link: https://doi.org/10.1111/..
 
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8

Exome sequencing reveals predominantly de novo variants in ..:

Järvelä, Irma ; Määttä, Tuomo ; Acharya, Anushree...
Human Genetics.  140 (2021)  7 - p. 1011-1029 , 2021
Link: https://doi.org/10.1007/..
 
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9

Phenotypic and Imaging Spectrum Associated With WDR45:

Adang, Laura A. ; Pizzino, Amy ; Malhotra, Alka...
Pediatric Neurology.  109 (2020)  - p. 56-62 , 2020
Link: https://doi.org/10.1016/..
 
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10

The spectrum of intermediate SCN8A‐related epilepsy:

Johannesen, Katrine M. ; Gardella, Elena ; Encinas, Alejandra C....
Epilepsia.  60 (2019)  5 - p. 830-844 , 2019
Link: https://doi.org/10.1111/..
 
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11

Defining the phenotypic spectrum of SLC6A1 mutations:

Johannesen, Katrine M. ; Gardella, Elena ; Linnankivi, Tarja...
Epilepsia.  59 (2018)  2 - p. 389-402 , 2018
Link: https://doi.org/10.1111/..
 
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12

De novo variants in neurodevelopmental disorders with epile..:

EuroEPINOMICS RES Consortium ; Heyne, Henrike O. ; Singh, Tarjinder...
Nature Genetics.  50 (2018)  7 - p. 1048-1053 , 2018
Link: https://doi.org/10.1038/..
 
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13

De Novo Mutations in Synaptic Transmission Genes Including ..:

Appenzeller, Silke ; Balling, Rudi ; Barisic, Nina...
The American Journal of Human Genetics.  100 (2017)  1 - p. 179 , 2017
Link: https://doi.org/10.1016/..
 
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14

De novo loss- or gain-of-function mutations in KCNA2 cause ..:

EuroEPINOMICS RES ; Syrbe, Steffen ; Hedrich, Ulrike B S...
Nature Genetics.  47 (2015)  4 - p. 393-399 , 2015
Link: https://doi.org/10.1038/..
 
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15

Selenoprotein biosynthesis defect causes progressive enceph..:

Anttonen, Anna-Kaisa ; Hilander, Taru ; Linnankivi, Tarja...
Neurology.  85 (2015)  4 - p. 306-315 , 2015
Link: https://doi.org/10.1212/..
 
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